Unotech Diagnostics, Inc.
FDA 510(k) & PMA Approved Devices — 3 products
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Total Devices3
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K032987 | ACCUTEST HCG-COMBO MODEL,HCG-004, ACCUSTRIP HCG-COMBO MODEL, HCG-005 | JHI | 2003-11-17 | View |
| 510(k) | K981838 | ACCUSTRIP HCG-URINE MODEL NUMBER HCG-002 | JHI | 1998-06-25 | View |
| 510(k) | K971886 | ACCUTEST HCG-URINE | JHI | 1997-06-11 | View |
No matching devices.
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